Veterinary Drugs Control Act Article 29
Regarding substandard veterinary drugs uncovered under this Act, if it is manufactured domestically and – upon inspection – can be modified and manufactured usable, the special municipal or county (city) competent authority shall dispatch personnel to supervise the original manufacturer to modify the drug before a set deadline. If the drugs concerned is imported with approval, the authority shall have it sealed and put in custody while the central competent authority orders the importer to initiate a goods-for-return process with the original overseas manufacturer.
中文原文 動物用藥品管理法第29條
依本法查獲之動物用劣藥，如係本國製造，經檢驗後仍可改製使用者，應由直轄市或縣（市）主管機關派員監督製造廠商限期改製；如係核准輸入者，應即封存，並由中央主管機關飭令原進口商限期向國外原廠商請求退貨。